Controlling Microstructure–Transport Interplay in Highly Phase-Separated Perfluorosulfonated Aromatic Multiblock Ionomers via Molecular Architecture Design - Université Grenoble Alpes Accéder directement au contenu
Article Dans Une Revue ACS Applied Materials & Interfaces Année : 2017

Controlling Microstructure–Transport Interplay in Highly Phase-Separated Perfluorosulfonated Aromatic Multiblock Ionomers via Molecular Architecture Design

Résumé

Proton-conducting multiblock polysulfones bearing perfluorosulfonic acid side chains were designed to encode nanoscale phase-separation, well-defined hydrophilic/hydrophobic interfaces, and optimized transport properties. Herein, we show that the superacid side chains yield highly ordered morphologies that can be tailored by best compromising ion-exchange capacity and block lengths. The obtained microstructures were extensively characterized by small-angle neutron scattering (SANS) over an extended range of hydration. Peculiar swelling behaviors were evidenced at two different scales and attributed to the dilution of locally flat polymer particles. We evidence the direct correlation between the quality of interfaces, the topology and connectivity of ionic nanodomains, the block superstructure long-range organization, and the transport properties. In particular, we found that the proton conductivity linearly depends on the microscopic expansion of both ionic and block domains. These findings indicate that neat nanoscale phase-separation and block-induced long-range connectivity can be optimized by designing aromatic ionomers with controlled architectures to improve the performances of polymer electrolyte membranes.
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Dates et versions

hal-03177437 , version 1 (23-03-2021)

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Citer

Huu-Dat Nguyen, Luca Assumma, Patrick Judeinstein, Regis Mercier, Lionel Porcar, et al.. Controlling Microstructure–Transport Interplay in Highly Phase-Separated Perfluorosulfonated Aromatic Multiblock Ionomers via Molecular Architecture Design. ACS Applied Materials & Interfaces, 2017, 9 (2), pp.1671-1683. ⟨10.1021/acsami.6b12764⟩. ⟨hal-03177437⟩
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